Login Preferences
About News Publications Statistics Downloads API Guide License How to use Preferences
bn:02945169n
Noun Concept
JA
No term available
EN
Harderoporphyria is a rare disorder of heme biosynthesis, inherited in an autosomal recessive manner caused by specific mutations in the CPOX gene. Wikipedia
Relations
Sources
IS A
ポルフィリン症

Please note that, in order to improve your browsing experience on this website, BabelNet® uses various types of cookies, including: browsing functionality, performance and statistical cookies.

By continuing to browse the site you are agreeing to our use of cookies. OK

License